FDA Application
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NDC Search Results on Active Ingredient: ibuprofen
Click on Active Ingredient to view the label.
Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
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IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 63941-166-16 | Valu Merchandisers Company (Best Choice) | ANDA090397 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 58602-814-10 | Aurohealth LLC | ANDA210676 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 49035-670-15 | Wal-Mart Stores, Inc. | ANDA090397 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 58602-814-18 | Aurohealth LLC | ANDA210676 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 30142-232-78 | KROGER COMPANY | ANDA090397 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; DIPHENHYDRAMINE HYDROCHLORIDE | 30142-232-15 | KROGER COMPANY | ANDA090397 | HUMAN OTC DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 43602-544-05 | Ascent Pharmaceuticals, Inc. | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-05 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 75987-010-03 | Horizon Therapeutics USA, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; FAMOTIDINE | 67877-626-01 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 67877-626-06 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 43602-544-30 | Ascent Pharmaceuticals, Inc. | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 63629-8891-2 | Bryant Ranch Prepack | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 0093-8107-98 | Teva Pharmaceuticals USA, Inc. | ANDA211278 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 43602-544-90 | Ascent Pharmaceuticals, Inc. | ANDA216814 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 70748-312-09 | Lupin Pharmaceuticals, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
IBUPROFEN; FAMOTIDINE | 63629-8891-1 | Bryant Ranch Prepack | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 63629-8891-3 | Bryant Ranch Prepack | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; FAMOTIDINE | 75987-010-72 | Horizon Therapeutics USA, Inc. | NDA022519 | HUMAN PRESCRIPTION DRUG | NDA |
IBUPROFEN; FAMOTIDINE | 67877-626-90 | Ascend Laboratories, LLC | ANDA211890 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 68084-841-01 | American Health Packaging | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 67296-1282-5 | RedPharm Drug, Inc. | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 33261-378-10 | Aidarex Pharmaceuticals LLC | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 68084-841-11 | American Health Packaging | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 33261-378-30 | Aidarex Pharmaceuticals LLC | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 53746-145-01 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 33261-378-90 | Aidarex Pharmaceuticals LLC | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 33261-378-60 | Aidarex Pharmaceuticals LLC | ANDA076604 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 53746-145-05 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
IBUPROFEN; HYDROCODONE BITARTRATE | 53746-117-01 | Amneal Pharmaceuticals of New York LLC | ANDA076642 | HUMAN PRESCRIPTION DRUG | ANDA |
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